(Q36918154)

17 August 2017

Discordant Haplotype Sequencing Identifies Functional Variants at the 2q33 Breast Cancer Risk Locus (English)

1 reference

17 August 2017

20

Lisa Cannon-Albright

0 references

Rosalie G Waller

Rosalie G Waller

7

0 references

Sushila H Rigas

Sushilaben H Rigas

8

0 references

Jason Gertz

Jason Gertz

25

0 references

Stacey Knight

Stacey Knight

21

0 references

Angela Cox

26

Angela Cox

1 reference

17 August 2017

24

Malcolm W R Reed

1 reference

17 August 2017

5

Timothy L Mosbruger

1 reference

17 August 2017

1

Nicola J Camp

1 reference

17 August 2017

Wei-Yu Lin

2

1 reference

17 August 2017

Alex Bigelow

3

1 reference

17 August 2017

George J Burghel

4

1 reference

17 August 2017

Marina A Parry

6

1 reference

17 August 2017

Pei-Yi Tai

9

1 reference

17 August 2017

Kristofer Berrett

10

1 reference

17 August 2017

Venkatesh Rajamanickam

11

1 reference

17 August 2017

Rachel Cosby

12

1 reference

17 August 2017

Ian W Brock

13

1 reference

17 August 2017

Brandt Jones

14

1 reference

17 August 2017

Dan Connley

15

1 reference

17 August 2017

Robert Sargent

16

1 reference

17 August 2017

Guoying Wang

17

1 reference

17 August 2017

Rachel E Factor

18

1 reference

17 August 2017

Philip S Bernard

19

1 reference

17 August 2017

Ryan Abo

22

1 reference

17 August 2017

Theresa L Werner

23

1 reference

17 August 2017

language of work or name

English

0 references

publication date

21 January 2016

1 reference

17 August 2017

1 reference

17 August 2017

76

1 reference

17 August 2017

7

1 reference

17 August 2017

1916-1925

1 reference

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Genetic and epigenetic fine mapping of causal autoimmune disease variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Defining the role of common variation in the genomic and biological architecture of adult human height

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Obesity-associated variants within FTO form long-range functional connections with IRX3

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Discovery and saturation analysis of cancer genes across 21 tumour types

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Systematic identification of trans eQTLs as putative drivers of known disease associations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Calculating sample size estimates for RNA sequencing data.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

ENCODE data in the UCSC Genome Browser: year 5 update

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

An integrated encyclopedia of DNA elements in the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

The landscape of cancer genes and mutational processes in breast cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Extensive promoter-centered chromatin interactions provide a topological basis for transcription regulation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Fine-mapping CASP8 risk variants in breast cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

A framework for variation discovery and genotyping using next-generation DNA sequencing data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Haplotype association analyses in resources of mixed structure using Monte Carlo testing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

The NIH Roadmap Epigenomics Mapping Consortium

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Genome-wide association study identifies five new breast cancer susceptibility loci

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Empirical methods for controlling false positives and estimating confidence in ChIP-Seq peaks

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

A freely diffusible form of Sonic hedgehog mediates long-range signalling

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

Initial sequencing and analysis of the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

A human cell line from a pleural effusion derived from a breast carcinoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

hapConstructor: automatic construction and testing of haplotypes in a Monte Carlo framework

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

A common coding variant in CASP8 is associated with breast cancer risk

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4873429

10.1158/0008-5472.CAN-15-1629

4 December 2018

Identifiers

DOI

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

26795348

1 reference